(2S,3R)-2-Acetamido-3-hydroxybutanoic acid

≥95%

Reagent Code: #233052
label
Alias N-acetyl-L-threonine; acetyl-L-threonine; acetyl-L-threonine; N-acetyl-L-threonine
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CAS Number 17093-74-2

science Other reagents with same CAS 17093-74-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 161.16 g/mol
Formula C₆H₁₁NO₄
badge Registry Numbers
MDL Number MFCD00037810
thermostat Physical Properties
Melting Point 125-128 °C
Boiling Point 443.3±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.275±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used in the synthesis of pharmaceuticals, particularly as an intermediate in the production of antiviral and anticancer agents. Its chiral structure makes it valuable in asymmetric synthesis, where stereochemistry plays a critical role in drug efficacy. Also employed in the development of enzyme inhibitors due to its structural similarity to natural metabolic intermediates. Commonly utilized in research settings for designing bioactive molecules and peptidomimetics.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,100.00
inventory 250mg
10-20 days ฿6,660.00
inventory 1g
10-20 days ฿20,500.00

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(2S,3R)-2-Acetamido-3-hydroxybutanoic acid
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Used in the synthesis of pharmaceuticals, particularly as an intermediate in the production of antiviral and anticancer agents. Its chiral structure makes it valuable in asymmetric synthesis, where stereochemistry plays a critical role in drug efficacy. Also employed in the development of enzyme inhibitors due to its structural similarity to natural metabolic intermediates. Commonly utilized in research settings for designing bioactive molecules and peptidomimetics.

Used in the synthesis of pharmaceuticals, particularly as an intermediate in the production of antiviral and anticancer agents. Its chiral structure makes it valuable in asymmetric synthesis, where stereochemistry plays a critical role in drug efficacy. Also employed in the development of enzyme inhibitors due to its structural similarity to natural metabolic intermediates. Commonly utilized in research settings for designing bioactive molecules and peptidomimetics.

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